Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca7 |
T |
G |
10: 79,838,848 (GRCm39) |
W674G |
probably damaging |
Het |
Abcc9 |
G |
A |
6: 142,638,606 (GRCm39) |
H103Y |
probably damaging |
Het |
Ano7 |
A |
G |
1: 93,323,224 (GRCm39) |
N495S |
probably null |
Het |
Aoc1l3 |
T |
A |
6: 48,964,965 (GRCm39) |
D324E |
probably benign |
Het |
Ash1l |
A |
G |
3: 88,889,584 (GRCm39) |
N488D |
probably benign |
Het |
Astn2 |
A |
G |
4: 65,563,119 (GRCm39) |
|
probably benign |
Het |
Atraid |
T |
A |
5: 31,209,796 (GRCm39) |
|
probably benign |
Het |
Baz2b |
T |
C |
2: 59,767,083 (GRCm39) |
R866G |
probably damaging |
Het |
Cep164 |
T |
A |
9: 45,688,234 (GRCm39) |
|
probably benign |
Het |
Clec4f |
G |
A |
6: 83,629,776 (GRCm39) |
Q261* |
probably null |
Het |
Cpne4 |
A |
T |
9: 104,563,640 (GRCm39) |
N6Y |
probably damaging |
Het |
Dhx38 |
G |
T |
8: 110,289,293 (GRCm39) |
Q36K |
probably benign |
Het |
Dna2 |
C |
A |
10: 62,793,910 (GRCm39) |
Q341K |
probably benign |
Het |
Dynap |
A |
G |
18: 70,375,165 (GRCm39) |
|
probably benign |
Het |
Eif3l |
T |
C |
15: 78,973,809 (GRCm39) |
V408A |
probably benign |
Het |
Foxi3 |
T |
A |
6: 70,934,122 (GRCm39) |
I203N |
probably damaging |
Het |
Gcc2 |
T |
A |
10: 58,134,511 (GRCm39) |
L1495Q |
probably damaging |
Het |
Gpr158 |
A |
G |
2: 21,830,019 (GRCm39) |
D688G |
probably damaging |
Het |
Hcfc2 |
C |
A |
10: 82,575,079 (GRCm39) |
T246K |
probably damaging |
Het |
Hdc |
C |
T |
2: 126,458,152 (GRCm39) |
E57K |
probably benign |
Het |
Iqsec3 |
G |
C |
6: 121,389,743 (GRCm39) |
|
probably benign |
Het |
Islr2 |
T |
A |
9: 58,106,645 (GRCm39) |
E205V |
probably damaging |
Het |
Klf9 |
T |
C |
19: 23,119,498 (GRCm39) |
L127P |
probably benign |
Het |
Lamc2 |
A |
T |
1: 152,999,840 (GRCm39) |
L1173Q |
probably damaging |
Het |
Lipe |
G |
A |
7: 25,097,901 (GRCm39) |
T14I |
possibly damaging |
Het |
Lnpep |
A |
G |
17: 17,751,394 (GRCm39) |
|
probably benign |
Het |
Lrrc15 |
A |
G |
16: 30,092,566 (GRCm39) |
S258P |
probably damaging |
Het |
Macc1 |
A |
T |
12: 119,410,780 (GRCm39) |
Y516F |
probably benign |
Het |
Megf6 |
A |
G |
4: 154,343,630 (GRCm39) |
T718A |
probably benign |
Het |
Mtcl2 |
A |
G |
2: 156,862,612 (GRCm39) |
L1439P |
probably damaging |
Het |
Myh1 |
A |
G |
11: 67,111,445 (GRCm39) |
D1628G |
probably damaging |
Het |
Naca |
C |
T |
10: 127,879,162 (GRCm39) |
T1398I |
probably benign |
Het |
Or1f12 |
A |
G |
13: 21,721,416 (GRCm39) |
F238S |
possibly damaging |
Het |
Or2a54 |
A |
T |
6: 43,093,150 (GRCm39) |
H158L |
possibly damaging |
Het |
Padi4 |
A |
G |
4: 140,496,740 (GRCm39) |
V52A |
possibly damaging |
Het |
Paqr5 |
G |
A |
9: 61,863,527 (GRCm39) |
T251I |
probably damaging |
Het |
Pcm1 |
A |
G |
8: 41,768,967 (GRCm39) |
D1611G |
probably damaging |
Het |
Prss12 |
G |
A |
3: 123,276,445 (GRCm39) |
R358K |
probably benign |
Het |
Racgap1 |
A |
T |
15: 99,526,587 (GRCm39) |
H325Q |
probably damaging |
Het |
Rc3h1 |
A |
T |
1: 160,795,228 (GRCm39) |
N1076I |
probably damaging |
Het |
Rp1 |
A |
G |
1: 4,415,088 (GRCm39) |
L2008P |
possibly damaging |
Het |
Rsph3a |
A |
G |
17: 8,164,919 (GRCm39) |
H93R |
possibly damaging |
Het |
Sbf1 |
C |
T |
15: 89,172,915 (GRCm39) |
R1840H |
probably damaging |
Het |
Skic8 |
T |
A |
9: 54,630,219 (GRCm39) |
|
probably benign |
Het |
Sytl2 |
T |
C |
7: 90,052,228 (GRCm39) |
|
probably benign |
Het |
Tbc1d9 |
T |
C |
8: 83,937,085 (GRCm39) |
S56P |
probably damaging |
Het |
Tiam2 |
A |
T |
17: 3,561,346 (GRCm39) |
M1304L |
probably damaging |
Het |
Tmprss11b |
G |
T |
5: 86,819,753 (GRCm39) |
R9S |
probably damaging |
Het |
Tnfrsf21 |
T |
A |
17: 43,348,505 (GRCm39) |
I39N |
probably benign |
Het |
Tnrc6b |
T |
C |
15: 80,763,604 (GRCm39) |
S369P |
probably benign |
Het |
Tpra1 |
T |
C |
6: 88,887,372 (GRCm39) |
V217A |
probably benign |
Het |
Uckl1 |
G |
C |
2: 181,212,283 (GRCm39) |
|
probably benign |
Het |
Vmn1r199 |
A |
T |
13: 22,566,736 (GRCm39) |
Q10L |
probably benign |
Het |
Vmn2r76 |
A |
G |
7: 85,879,506 (GRCm39) |
S265P |
possibly damaging |
Het |
Vwa5b1 |
A |
T |
4: 138,321,662 (GRCm39) |
L377Q |
probably damaging |
Het |
Wrap73 |
A |
G |
4: 154,229,776 (GRCm39) |
D49G |
probably damaging |
Het |
Zfp764 |
T |
A |
7: 127,004,051 (GRCm39) |
Q360L |
possibly damaging |
Het |
Zfp846 |
G |
A |
9: 20,499,224 (GRCm39) |
|
probably benign |
Het |
Zranb2 |
T |
C |
3: 157,240,096 (GRCm39) |
I14T |
probably benign |
Het |
|
Other mutations in Rbm12b1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00953:Rbm12b1
|
APN |
4 |
12,146,038 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02103:Rbm12b1
|
APN |
4 |
12,145,563 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03165:Rbm12b1
|
APN |
4 |
12,145,845 (GRCm39) |
missense |
possibly damaging |
0.94 |
PIT4618001:Rbm12b1
|
UTSW |
4 |
12,145,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R0449:Rbm12b1
|
UTSW |
4 |
12,145,507 (GRCm39) |
missense |
probably benign |
0.00 |
R0571:Rbm12b1
|
UTSW |
4 |
12,146,248 (GRCm39) |
missense |
probably benign |
0.00 |
R1476:Rbm12b1
|
UTSW |
4 |
12,145,817 (GRCm39) |
missense |
possibly damaging |
0.74 |
R1709:Rbm12b1
|
UTSW |
4 |
12,145,827 (GRCm39) |
missense |
probably benign |
0.00 |
R1759:Rbm12b1
|
UTSW |
4 |
12,145,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R1967:Rbm12b1
|
UTSW |
4 |
12,146,304 (GRCm39) |
missense |
probably benign |
0.00 |
R2055:Rbm12b1
|
UTSW |
4 |
12,145,606 (GRCm39) |
missense |
probably benign |
0.05 |
R2425:Rbm12b1
|
UTSW |
4 |
12,146,443 (GRCm39) |
missense |
probably damaging |
0.99 |
R4015:Rbm12b1
|
UTSW |
4 |
12,145,491 (GRCm39) |
missense |
probably benign |
0.04 |
R4332:Rbm12b1
|
UTSW |
4 |
12,145,655 (GRCm39) |
missense |
probably benign |
0.02 |
R5773:Rbm12b1
|
UTSW |
4 |
12,145,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R6497:Rbm12b1
|
UTSW |
4 |
12,146,431 (GRCm39) |
missense |
probably benign |
0.00 |
R7740:Rbm12b1
|
UTSW |
4 |
12,145,954 (GRCm39) |
missense |
probably benign |
0.00 |
R7761:Rbm12b1
|
UTSW |
4 |
12,146,460 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8083:Rbm12b1
|
UTSW |
4 |
12,146,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R8129:Rbm12b1
|
UTSW |
4 |
12,145,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R8389:Rbm12b1
|
UTSW |
4 |
12,146,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R8932:Rbm12b1
|
UTSW |
4 |
12,145,689 (GRCm39) |
missense |
probably benign |
0.00 |
R9302:Rbm12b1
|
UTSW |
4 |
12,146,181 (GRCm39) |
missense |
probably benign |
0.13 |
Z1088:Rbm12b1
|
UTSW |
4 |
12,146,079 (GRCm39) |
missense |
probably benign |
|
|